JP2018526379A - リン含有シアノヒドリンエステルの製造方法 - Google Patents

リン含有シアノヒドリンエステルの製造方法 Download PDF

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Publication number: JP2018526379A
Authority: JP; Japan
Prior art keywords: formula; mol; weight; compound; metering
Prior art date: 2015-09-02
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Pending

Application number

JP2018511191A

Other languages

English (en)

Japanese (ja)

Inventor

レッセル，ハンス−ヨアヒム

テルマン，キリアン

フォード，マルク・ジェイムズ

リットマン，マルティン

シュレーゲル，ギュンター

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Bayer CropScience AG

Original Assignee

Bayer CropScience AG

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2015-09-02

Filing date

2016-08-29

Publication date

2018-09-13

2016-08-29 Application filed by Bayer CropScience AG filed Critical Bayer CropScience AG

2018-09-13 Publication of JP2018526379A publication Critical patent/JP2018526379A/ja

Status Pending legal-status Critical Current

Links

238000004519 manufacturing process Methods 0.000 title claims description 14
150000002148 esters Chemical class 0.000 title abstract description 34
229910052698 phosphorus Inorganic materials 0.000 title abstract description 21
239000011574 phosphorus Substances 0.000 title abstract description 21
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 title abstract description 20
238000000034 method Methods 0.000 claims abstract description 98
IAJOBQBIJHVGMQ-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid Chemical compound CP(O)(=O)CCC(N)C(O)=O IAJOBQBIJHVGMQ-UHFFFAOYSA-N 0.000 claims abstract description 58
239000005561 Glufosinate Substances 0.000 claims abstract description 34
238000002360 preparation method Methods 0.000 claims abstract description 24
239000000126 substance Substances 0.000 claims abstract description 15
150000001875 compounds Chemical class 0.000 claims description 126
150000003254 radicals Chemical class 0.000 claims description 77
238000006243 chemical reaction Methods 0.000 claims description 60
KQYLUTYUZIVHND-UHFFFAOYSA-N tert-butyl 2,2-dimethyloctaneperoxoate Chemical compound CCCCCCC(C)(C)C(=O)OOC(C)(C)C KQYLUTYUZIVHND-UHFFFAOYSA-N 0.000 claims description 28
125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 26
-1 1,1, 3,3-tetramethylbutyl Chemical group 0.000 claims description 26
239000000203 mixture Substances 0.000 claims description 26
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 17
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 16
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 14
239000002253 acid Substances 0.000 claims description 14
239000001257 hydrogen Substances 0.000 claims description 14
229910052739 hydrogen Inorganic materials 0.000 claims description 14
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 10
125000000008 (C1-C10) alkyl group Chemical group 0.000 claims description 6
125000004400 (C1-C12) alkyl group Chemical group 0.000 claims description 6
125000004641 (C1-C12) haloalkyl group Chemical group 0.000 claims description 6
125000006546 (C4-C10) cycloalkyl group Chemical group 0.000 claims description 6
125000000041 C6-C10 aryl group Chemical group 0.000 claims description 6
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 6
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
229910052708 sodium Inorganic materials 0.000 claims description 6
239000011734 sodium Substances 0.000 claims description 6
125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 5
RAWISQFSQWIXCW-UHFFFAOYSA-N 2-methylbutan-2-yl 2,2-dimethyloctaneperoxoate Chemical compound CCCCCCC(C)(C)C(=O)OOC(C)(C)CC RAWISQFSQWIXCW-UHFFFAOYSA-N 0.000 claims description 5
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 5
DUVTXUGBACWHBP-UHFFFAOYSA-N methyl 2-(1h-benzimidazol-2-ylmethoxy)benzoate Chemical compound COC(=O)C1=CC=CC=C1OCC1=NC2=CC=CC=C2N1 DUVTXUGBACWHBP-UHFFFAOYSA-N 0.000 claims description 5
OPQYOFWUFGEMRZ-UHFFFAOYSA-N tert-butyl 2,2-dimethylpropaneperoxoate Chemical compound CC(C)(C)OOC(=O)C(C)(C)C OPQYOFWUFGEMRZ-UHFFFAOYSA-N 0.000 claims description 5
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
125000005347 halocycloalkyl group Chemical group 0.000 claims description 3
125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 3
239000001301 oxygen Substances 0.000 claims description 3
229910052760 oxygen Inorganic materials 0.000 claims description 3
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
229910052717 sulfur Chemical group 0.000 claims description 2
239000011593 sulfur Chemical group 0.000 claims description 2
HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 34
239000003999 initiator Substances 0.000 description 19
239000000376 reactant Substances 0.000 description 14
125000000217 alkyl group Chemical group 0.000 description 7
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
239000000047 product Substances 0.000 description 6
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 5
0 CC(C)(*)C(CCC(C)(*)Cl)=* Chemical compound CC(C)(*)C(CCC(C)(*)Cl)=* 0.000 description 4
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 4
230000015572 biosynthetic process Effects 0.000 description 4
125000004432 carbon atom Chemical group C* 0.000 description 4
239000007795 chemical reaction product Substances 0.000 description 4
230000000052 comparative effect Effects 0.000 description 4
239000003085 diluting agent Substances 0.000 description 4
208000028659 discharge Diseases 0.000 description 4
229910052731 fluorine Inorganic materials 0.000 description 4
125000001188 haloalkyl group Chemical group 0.000 description 4
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
239000000460 chlorine Substances 0.000 description 3
238000010924 continuous production Methods 0.000 description 3
238000002474 experimental method Methods 0.000 description 3
239000011737 fluorine Substances 0.000 description 3
229910052757 nitrogen Inorganic materials 0.000 description 3
238000000746 purification Methods 0.000 description 3
AZUYLZMQTIKGSC-UHFFFAOYSA-N 1-[6-[4-(5-chloro-6-methyl-1H-indazol-4-yl)-5-methyl-3-(1-methylindazol-5-yl)pyrazol-1-yl]-2-azaspiro[3.3]heptan-2-yl]prop-2-en-1-one Chemical compound ClC=1C(=C2C=NNC2=CC=1C)C=1C(=NN(C=1C)C1CC2(CN(C2)C(C=C)=O)C1)C=1C=C2C=NN(C2=CC=1)C AZUYLZMQTIKGSC-UHFFFAOYSA-N 0.000 description 2
XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
OGBVRMYSNSKIEF-UHFFFAOYSA-N Benzylphosphonic acid Chemical compound OP(O)(=O)CC1=CC=CC=C1 OGBVRMYSNSKIEF-UHFFFAOYSA-N 0.000 description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
239000003905 agrochemical Substances 0.000 description 2
UOKRBSXOBUKDGE-UHFFFAOYSA-N butylphosphonic acid Chemical compound CCCCP(O)(O)=O UOKRBSXOBUKDGE-UHFFFAOYSA-N 0.000 description 2
239000006227 byproduct Substances 0.000 description 2
SHZIWNPUGXLXDT-UHFFFAOYSA-N caproic acid ethyl ester Natural products CCCCCC(=O)OCC SHZIWNPUGXLXDT-UHFFFAOYSA-N 0.000 description 2
229910052801 chlorine Inorganic materials 0.000 description 2
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
230000008878 coupling Effects 0.000 description 2
238000010168 coupling process Methods 0.000 description 2
238000005859 coupling reaction Methods 0.000 description 2
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
GATNOFPXSDHULC-UHFFFAOYSA-N ethylphosphonic acid Chemical compound CCP(O)(O)=O GATNOFPXSDHULC-UHFFFAOYSA-N 0.000 description 2
239000007789 gas Substances 0.000 description 2
239000011521 glass Substances 0.000 description 2
230000002363 herbicidal effect Effects 0.000 description 2
239000000543 intermediate Substances 0.000 description 2
YACKEPLHDIMKIO-UHFFFAOYSA-N methylphosphonic acid Chemical compound CP(O)(O)=O YACKEPLHDIMKIO-UHFFFAOYSA-N 0.000 description 2
238000002156 mixing Methods 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
NSETWVJZUWGCKE-UHFFFAOYSA-N propylphosphonic acid Chemical compound CCCP(O)(O)=O NSETWVJZUWGCKE-UHFFFAOYSA-N 0.000 description 2
230000001681 protective effect Effects 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
238000003756 stirring Methods 0.000 description 2
238000003786 synthesis reaction Methods 0.000 description 2
125000004765 (C1-C4) haloalkyl group Chemical group 0.000 description 1
125000006529 (C3-C6) alkyl group Chemical group 0.000 description 1
OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 1
MEHLEOUIWVWVBF-UHFFFAOYSA-N 1-cyanoprop-2-enyl acetate Chemical compound CC(=O)OC(C=C)C#N MEHLEOUIWVWVBF-UHFFFAOYSA-N 0.000 description 1
RUNJHCZDNSMWGF-UHFFFAOYSA-N 1-propylphosphonoylpropane Chemical compound CCCP(=O)CCC RUNJHCZDNSMWGF-UHFFFAOYSA-N 0.000 description 1
MPDAXLBCFBEPOU-UHFFFAOYSA-N 2,4,4-trimethylpentan-2-yl 2-ethylhexanoate Chemical compound CCCCC(CC)C(=O)OC(C)(C)CC(C)(C)C MPDAXLBCFBEPOU-UHFFFAOYSA-N 0.000 description 1
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
DFZNUSYMRMOKBK-UHFFFAOYSA-N C.OPO Chemical class C.OPO DFZNUSYMRMOKBK-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
YFPJFKYCVYXDJK-UHFFFAOYSA-N Diphenylphosphine oxide Chemical compound C=1C=CC=CC=1[P+](=O)C1=CC=CC=C1 YFPJFKYCVYXDJK-UHFFFAOYSA-N 0.000 description 1
FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
229910052784 alkaline earth metal Inorganic materials 0.000 description 1
150000001413 amino acids Chemical class 0.000 description 1
150000003863 ammonium salts Chemical class 0.000 description 1
229910052786 argon Inorganic materials 0.000 description 1
125000003710 aryl alkyl group Chemical group 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
238000010923 batch production Methods 0.000 description 1
230000000975 bioactive effect Effects 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
125000001246 bromo group Chemical group Br* 0.000 description 1
PKVYRMYNUBUIJI-UHFFFAOYSA-N butoxy(methyl)phosphinous acid Chemical compound CCCCOP(C)O PKVYRMYNUBUIJI-UHFFFAOYSA-N 0.000 description 1
ISWZIPFYROHEQV-UHFFFAOYSA-N butylphosphonous acid Chemical compound CCCCP(O)O ISWZIPFYROHEQV-UHFFFAOYSA-N 0.000 description 1
ACLBAKCXXIZYJV-UHFFFAOYSA-N chembl1463773 Chemical compound C=1C=CC=CC=1CP(=O)CC1=CC=CC=C1 ACLBAKCXXIZYJV-UHFFFAOYSA-N 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
238000001816 cooling Methods 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
JMCNGFNJWDJIIV-UHFFFAOYSA-N dibutyl(oxo)phosphanium Chemical compound CCCC[P+](=O)CCCC JMCNGFNJWDJIIV-UHFFFAOYSA-N 0.000 description 1
229940117389 dichlorobenzene Drugs 0.000 description 1
YVXVNGVYXSQARS-UHFFFAOYSA-N diethyl(oxo)phosphanium Chemical compound CC[P+](=O)CC YVXVNGVYXSQARS-UHFFFAOYSA-N 0.000 description 1
125000004982 dihaloalkyl group Chemical group 0.000 description 1
WQAWEUZTDVWTDB-UHFFFAOYSA-N dimethyl(oxo)phosphanium Chemical compound C[P+](C)=O WQAWEUZTDVWTDB-UHFFFAOYSA-N 0.000 description 1
TZANYKYQDDZSQZ-UHFFFAOYSA-N dimethyl(sulfanylidene)-lambda5-phosphane Chemical compound CP(C)=S TZANYKYQDDZSQZ-UHFFFAOYSA-N 0.000 description 1
CHYUXCABJMXHJN-UHFFFAOYSA-N diphenyl(sulfanylidene)phosphanium Chemical compound C=1C=CC=CC=1[P+](=S)C1=CC=CC=C1 CHYUXCABJMXHJN-UHFFFAOYSA-N 0.000 description 1
238000007323 disproportionation reaction Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
230000005684 electric field Effects 0.000 description 1
238000002848 electrochemical method Methods 0.000 description 1
230000005672 electromagnetic field Effects 0.000 description 1
WFSUZRTZCVKBFF-UHFFFAOYSA-N ethane phosphonous acid Chemical compound P(O)O.CC WFSUZRTZCVKBFF-UHFFFAOYSA-N 0.000 description 1
238000011049 filling Methods 0.000 description 1
IAJOBQBIJHVGMQ-BYPYZUCNSA-N glufosinate-P Chemical compound CP(O)(=O)CC[C@H](N)C(O)=O IAJOBQBIJHVGMQ-BYPYZUCNSA-N 0.000 description 1
125000003106 haloaryl group Chemical group 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
VQKMAVKPNBDWLK-UHFFFAOYSA-N hydroxy-methyl-phenoxy-sulfanylidene-lambda5-phosphane Chemical compound CP(O)(=S)Oc1ccccc1 VQKMAVKPNBDWLK-UHFFFAOYSA-N 0.000 description 1
230000002779 inactivation Effects 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
239000011630 iodine Substances 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
238000002955 isolation Methods 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
238000011068 loading method Methods 0.000 description 1
239000000463 material Substances 0.000 description 1
238000010327 methods by industry Methods 0.000 description 1
MUQLDUAEMOVCOY-UHFFFAOYSA-N methyl(sulfanyl)phosphinous acid Chemical compound CP(O)S MUQLDUAEMOVCOY-UHFFFAOYSA-N 0.000 description 1
PMVVRSKJCGEFIY-UHFFFAOYSA-N methylphosphonous acid Chemical compound CP(O)O PMVVRSKJCGEFIY-UHFFFAOYSA-N 0.000 description 1
ATPGNTDARNWVLL-UHFFFAOYSA-N methylphosphonoylbenzene Chemical compound CP(=O)C1=CC=CC=C1 ATPGNTDARNWVLL-UHFFFAOYSA-N 0.000 description 1
125000006682 monohaloalkyl group Chemical group 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
238000006384 oligomerization reaction Methods 0.000 description 1
MSVORCUEJCHPKS-UHFFFAOYSA-N phenoxy(phenyl)phosphinic acid Chemical compound C=1C=CC=CC=1P(=O)(O)OC1=CC=CC=C1 MSVORCUEJCHPKS-UHFFFAOYSA-N 0.000 description 1
CGNKSELPNJJTSM-UHFFFAOYSA-N phenylphosphonous acid Chemical compound OP(O)C1=CC=CC=C1 CGNKSELPNJJTSM-UHFFFAOYSA-N 0.000 description 1
150000004714 phosphonium salts Chemical class 0.000 description 1
XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical compound OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
MWBOOFOIEFTTHB-UHFFFAOYSA-N propylphosphonous acid Chemical compound CCCP(O)O MWBOOFOIEFTTHB-UHFFFAOYSA-N 0.000 description 1
230000005855 radiation Effects 0.000 description 1
239000002994 raw material Substances 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
238000005070 sampling Methods 0.000 description 1
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
238000007086 side reaction Methods 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
125000004385 trihaloalkyl group Chemical group 0.000 description 1
238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/30—Phosphinic acids [R2P(=O)(OH)]; Thiophosphinic acids ; [R2P(=X1)(X2H) (X1, X2 are each independently O, S or Se)]
- C07F9/32—Esters thereof
- C07F9/3205—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/3211—Esters of acyclic saturated acids which can have further substituents on alkyl
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds

Landscapes

Life Sciences & Earth Sciences (AREA)
Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
General Health & Medical Sciences (AREA)
Health & Medical Sciences (AREA)
Biochemistry (AREA)
Molecular Biology (AREA)
Dentistry (AREA)
Engineering & Computer Science (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Plant Pathology (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

JP2018511191A 2015-09-02 2016-08-29 リン含有シアノヒドリンエステルの製造方法 Pending JP2018526379A (ja)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
EP15183423.1		2015-09-02
EP15183423		2015-09-02
PCT/EP2016/070301 WO2017037009A1 (de)	2015-09-02	2016-08-29	Verfahren zur herstellung von phosphorhaltigen cyanhydrinestern

Publications (1)

Publication Number	Publication Date
JP2018526379A true JP2018526379A (ja)	2018-09-13

Family

ID=54062633

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP2018511191A Pending JP2018526379A (ja)	2015-09-02	2016-08-29	リン含有シアノヒドリンエステルの製造方法

Country Status (9)

Country	Link
US (1)	US10941167B2 (es)
EP (1)	EP3344635B1 (es)
JP (1)	JP2018526379A (es)
KR (1)	KR20180048661A (es)
CN (1)	CN108026122B (es)
IL (1)	IL257375A (es)
MX (1)	MX2018002729A (es)
TW (1)	TW201726693A (es)
WO (1)	WO2017037009A1 (es)

Families Citing this family (5)

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2016
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- 2016-08-29 EP EP16757668.5A patent/EP3344635B1/de active Active
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- 2016-08-29 CN CN201680050960.6A patent/CN108026122B/zh active Active
- 2016-08-29 KR KR1020187006004A patent/KR20180048661A/ko not_active Withdrawn
- 2016-08-29 WO PCT/EP2016/070301 patent/WO2017037009A1/de not_active Ceased
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Publication number	Publication date
US10941167B2 (en)	2021-03-09
US20180251481A1 (en)	2018-09-06
WO2017037009A1 (de)	2017-03-09
IL257375A (en)	2018-04-30
CN108026122B (zh)	2021-03-09
KR20180048661A (ko)	2018-05-10
MX2018002729A (es)	2018-04-13
EP3344635B1 (de)	2019-08-07
TW201726693A (zh)	2017-08-01
EP3344635A1 (de)	2018-07-11
CN108026122A (zh)	2018-05-11

Publication	Publication Date	Title
JP2018529662A (ja)	2018-10-11	リン含有シアノヒドリンエステルの製造方法
CA2948713C (en)	2023-04-04	Process for preparing phosphorus-containing cyanohydrins
JP2018526379A (ja)	2018-09-13	リン含有シアノヒドリンエステルの製造方法
CN108137628B (zh)	2020-10-09	制备含磷的氰醇酯的方法
JP2018529663A (ja)	2018-10-11	リンを含んでいるシアノヒドリンエステルを製造する方法

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